A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005658



Internal ID19094875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158545091..158556782hg38UCSC Ensembl
Innerchr1:158514881..158526572hg19UCSC Ensembl
Innerchr1:156781505..156793196hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3811692
hg1911692
hg1811692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv443n100
Supporting Variantsnssv3491267
Samples
Known GenesOR6Y1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005658
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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